17-beta-Hydroxy-5alpha-androst-1-en-3-one acetate

Base Information

Chemical Name:17-beta-Hydroxy-5alpha-androst-1-en-3-one acetate
CAS No.:64-82-4
Molecular Formula:C₂₁H₃₀O₃
Molecular Weight:330.467
Hs Code.:
European Community (EC) Number:200-595-9
DSSTox Substance ID:DTXSID60981907
Nikkaji Number:J213.550G
Mol file:64-82-4.mol

Synonyms:64-82-4;17-beta-Hydroxy-5alpha-androst-1-en-3-one acetate;EINECS 200-595-9;[(5S,8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] acetate;17beta-acetoxy-3-oxo-5alpha-androst-1-ene;SCHEMBL7196987;DTXSID60981907;NKZLRJOJLCHNQR-NGFSFWIMSA-N;3-Oxoandrost-1-en-17-yl acetate;17beta-acetoxy-5alpha-androst-1-en-3-one;17beta-(Acetyloxy)-5alpha-androst-1-en-3-one;17-beta-hydroxy-5alpha-androst-1-en-3-onacetat;Androst-1-en-3-one, 17-(acetyloxy)-, (5alpha,17beta)-

Suppliers and Price of 17-beta-Hydroxy-5alpha-androst-1-en-3-one acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 9 raw suppliers

Chemical Property of 17-beta-Hydroxy-5alpha-androst-1-en-3-one acetate

Chemical Property:

PSA：43.37000
LogP:4.30590
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:330.21949481
Heavy Atom Count:24
Complexity:594

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1CCC2C1(CCC3C2CCC4C3(C=CC(=O)C4)C)C
Isomeric SMILES:CC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC[C@@H]4[C@@]3(C=CC(=O)C4)C)C

Technology Process of 17-beta-Hydroxy-5alpha-androst-1-en-3-one acetate

There total 22 articles about 17-beta-Hydroxy-5alpha-androst-1-en-3-one acetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.6%

: 952222-37-6
(5S,8R,9S,10S,13S,14S,17S)-2-bromo-10,13-dimethyl-3-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate

: 64-82-4,6656-41-3,21507-42-6,25615-33-2,54631-35-5,79732-37-9,97413-69-9
(5α,17β)-3-oxoandrost-1-en-17-yl acetate

Guidance literature:: With lithium carbonate; lithium bromide; In N,N-dimethyl-formamide; for 0.5h; Heating;
DOI:10.1016/j.steroids.2006.09.008